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Relevant bibliographies by topics / Bis (2-chloroethyl) sulfide

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Journal articles

Academic literature on the topic 'Bis (2-chloroethyl) sulfide'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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Journal articles on the topic "Bis (2-chloroethyl) sulfide"

1

Tilley, RI. "Stability Constants of Silver(I) Complexes of Bis(2-chloroethyl) Sulfide (Sulfur Mustard) and Some Related Thioethers in Polar Organic Solvents." Australian Journal of Chemistry 43, no. 9 (1990): 1573. http://dx.doi.org/10.1071/ch9901573.

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Stability constants of complexes formed between silver(I) and diethyl sulfide, 2-chloroethyl ethyl sulfide and bis (2-chloroethyl) sulfide (sulfur mustard) in acetone, methanol, dimethylformamide and dimethyl sulfoxide have been determined. The reduced stability of silver(I) complexes with ligands containing a 2-chloroethyl group has been explained in terms of the sulfonium ion character of the ligands.

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2

Abuzalat, Osama, Setareh Homayoonnia, Danny Wong, Hesham R. Tantawy, and Seonghwan Kim. "Facile and rapid synthesis of functionalized Zr-BTC for the optical detection of the blistering agent simulant 2-chloroethyl ethyl sulfide (CEES)." Dalton Transactions 50, no. 9 (2021): 3261–68. http://dx.doi.org/10.1039/d0dt04382f.

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2-Chloroethyl ethyl sulfide (CEES) is a simulant for the chemical warfare agent, bis(2-chloroethyl) sulfide, also known as mustard gas. Functionalized Zr-BTC is synthesized and exploited for the optical detection of CEES.

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3

Buchanan, James H., Leonard C. Buettner, and David E. Tevault. "Vapor Pressure of Solid Bis(2-chloroethyl) Sulfide." Journal of Chemical & Engineering Data 51, no. 4 (2006): 1331–34. http://dx.doi.org/10.1021/je060077o.

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4

Wagner, George W., Brian K. Maciver, Dennis K. Rohrbaugh, and Yu-Chu Yang. "THERMAL DEGRADATION OF BIS (2-CHLOROETHYL) SULFIDE (MUSTARD GAS)." Phosphorus, Sulfur, and Silicon and the Related Elements 152, no. 1 (1999): 65–76. http://dx.doi.org/10.1080/10426509908031618.

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5

Vycudilik, W. "Detection of mustard gas bis(2-chloroethyl)-sulfide in urine." Forensic Science International 28, no. 2 (1985): 131–36. http://dx.doi.org/10.1016/0379-0738(85)90070-2.

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6

Voronkov, M. G., E. P. Levanova, E. N. Sukhomazova, N. V. Russavskaya, E. N. Deryagina, and N. A. Korchevin. "High-Temperature Synthesis of Thiophene from Bis(2-chloroethyl) Sulfide." Russian Journal of Organic Chemistry 41, no. 6 (2005): 891–93. http://dx.doi.org/10.1007/s11178-005-0260-5.

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7

Dubey, Vinita, S. N. Maiti, N. B. S. N. Rao, and A. K. Gupta. "Study of Permeation of Bis(2-Chloroethyl)Sulfide Through Elastomer Membranes." Polymer-Plastics Technology and Engineering 36, no. 3 (1997): 445–60. http://dx.doi.org/10.1080/03602559708000634.

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8

Eisenmenger, Wolfgang, Gustav Drasch, Max von Clarmann, Elisabeth Kretschmer, and Gabriele Roider. "Clinical and Morphological Findings on Mustard Gas [Bis(2-Chloroethyl)Sulfide] Poisoning." Journal of Forensic Sciences 36, no. 6 (1991): 13192J. http://dx.doi.org/10.1520/jfs13192j.

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9

Dubey, D. K., R. C. Malhotra, R. Vaidyanathaswamy, and R. Vijayaraghavan. "Reaction of Bis(2-chloroethyl) Sulfide withN,N‘-Dichlorobis(2,4,6-trichlorophenyl)urea." Journal of Organic Chemistry 64, no. 21 (1999): 8031–33. http://dx.doi.org/10.1021/jo990783a.

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10

Dillman, James F., Christopher S. Phillips, Linda M. Dorsch, et al. "Genomic Analysis of Rodent Pulmonary Tissue Following Bis-(2-chloroethyl) Sulfide Exposure." Chemical Research in Toxicology 18, no. 1 (2005): 28–34. http://dx.doi.org/10.1021/tx049745z.

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